Target Device 253671
by Fournitures Hospitalieres Industrie
Target Device 253671 is a Class II device made by Fournitures Hospitalieres Industrie, cleared under FDA 510(k) K033510 on 3 Dec 2003 (1 earlier submission) and listed in FDA GUDID since 13 Mar 2019 (UDI-DI 03661489536717), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03661489536717 | Date13 Mar 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK033510 | Date3 Dec 2003 | StatusActive |
Official records
- AccessGUDID record 03661489536717
- FDA 510(k) database K033510
- FDA 510(k) database K023241
Across registries
- FDA 510(k) K033510 decided 3 Dec 2003 Active
- FDA GUDID UDI-DI 03661489536717 listed 13 Mar 2019 Listed
Timeline
- Cleared FDA 510(k) K023241
- Cleared FDA 510(k) K033510
- Listed FDA GUDID 03661489536717
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Target Device
- Generic name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / reference
- 253671
- Primary DI / UDI-DI
- 03661489536717
- FDA product code
- HSB
- GMDN term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device class
- Class II
- Regulation number
- 888.3020
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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